- Ensure secondary assembly operations performed per SOP and PIC/S GMP applicable guidelines.
- Ensure sufficient PPM inventory level to ensure no disruption to secondary assembly operations.
- Responsible in creating Master Batch Packaging Record (MBPR) for Non-Pharmaceutical Products.
- Introduce process improvement relevant to second assembly operations.
- Housekeeping of redressing area.
- Responsible in performing 100% Incoming Quality Inspection for Pharmaceutical Trade Returned Products.
- Responsible in performing Sampling Incoming Quality Inspection & reporting based on Principal Artwork (as per Technical Agreement).
- Responsible in reporting and follow-up on non-conforming products (Inclusive of Incoming, Outgoing, Returns, 3PL and Redressing).
Interested candidates please send in your resume to:
Topaz Liang Huimin (CEI No. R1104500), email to: [Confidential Information]
EA License No: 99C4599
